nadolol

Generic: nadolol

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nadolol
Generic Name nadolol
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nadolol 20 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7070
Product ID 0904-7070_b21e6ce1-5758-40d6-8933-c2dc31255f2d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203455
Marketing Start 2016-02-23
Marketing End 2026-04-30

Pharmacologic Class

Established (EPC)
beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047070
Hyphenated Format 0904-7070

Supplemental Identifiers

RxCUI
198006 198007
UNII
FEN504330V
NUI
N0000000161 N0000175556

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nadolol (source: ndc)
Generic Name nadolol (source: ndc)
Application Number ANDA203455 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-7070-07) / 1 TABLET in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0904-7070-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

0904-7070-07 30 BLISTER PACK in 1 CARTON (0904-7070-07) / 1 TABLET in 1 BLISTER PACK 0904-7070-61 100 BLISTER PACK in 1 CARTON (0904-7070-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

nadolol (20 mg/1)

Linked Drug Pages (1)

Nadolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b21e6ce1-5758-40d6-8933-c2dc31255f2d", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007"], "spl_set_id": ["58ae7b7e-fa22-486b-9fa3-cfb31d81c637"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7070-07)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7070-07", "marketing_end_date": "20260430", "marketing_start_date": "20160223"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7070-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7070-61", "marketing_end_date": "20260430", "marketing_start_date": "20160223"}], "brand_name": "Nadolol", "product_id": "0904-7070_b21e6ce1-5758-40d6-8933-c2dc31255f2d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7070", "generic_name": "Nadolol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "20 mg/1"}], "application_number": "ANDA203455", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20160223"}